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Research 451–480 of 1000+
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Structural abnormalities of the hair shaft
- Hypertrichosis
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Critical Developmental Periods for Effects on Male Rat Genitalia Induced by Finasteride, a 5α-Reductase Inhibitor
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Acne as a chronic systemic disease
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- The clinical evaluation of hirsutism
- The Use of Micrografts and Minigrafts in the Aesthetic Reconstruction of the Face and Scalp
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Adverse Reactions to Oral Retinoids An Update
- Diagnostic Criteria for Polycystic Ovarian Syndrome
- Hirsutism: Diagnosis and management
- Vitamin D<sub>3</sub>Analogs Stimulate Hair Growth in Nude Mice
- Genetic hair and nail disorders
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Office Diagnosis of Hair Shaft Defects
- Premature Adrenarche
- Cardiovascular risk factors and events in women with androgen excess
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Hairless is a nuclear receptor corepressor essential for skin function
- What does acne genetics teach us about disease pathogenesis?
- Management of CAH during pregnancy
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Cholesterol homeostasis: Links to hair follicle biology and hair disorders
- Hair Loss in Children
- Hormone therapy in acne
- Hirsutism in the United Arab Emirates: a hospital study